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Mimicking pancreatic malignancy: a systemic sarcoidosis

Systemic sarcoidosis that initially presents as a pancreatic mass has rarely been reported. A 47-year-old man presented with idiopathic epigastric abdominal pain. Abdominal CT showed multiple enlarged lymph nodes in the retroperitoneal area and a suspected tumor mass in the pancreatic head region. T...

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Autores principales: Zhang, Li-Na, Xue, Qing-Liang, Wang, Jian-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074940/
https://www.ncbi.nlm.nih.gov/pubmed/24658558
http://dx.doi.org/10.5144/0256-4947.2014.70
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author Zhang, Li-Na
Xue, Qing-Liang
Wang, Jian-Xin
author_facet Zhang, Li-Na
Xue, Qing-Liang
Wang, Jian-Xin
author_sort Zhang, Li-Na
collection PubMed
description Systemic sarcoidosis that initially presents as a pancreatic mass has rarely been reported. A 47-year-old man presented with idiopathic epigastric abdominal pain. Abdominal CT showed multiple enlarged lymph nodes in the retroperitoneal area and a suspected tumor mass in the pancreatic head region. The preliminary diagnosis was celiac metastasis of a pancreatic malignancy. The definitive diagnosis was systemic sarcoidosis, which was supported by granulomas on histology, clinical radiographic findings, and clinical response to steroids. A review of published reports on sarcoidosis presenting initially as a pancreatic or celiac mass from the Chinese biomedical database (1978–2010) is included.
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spelling pubmed-60749402018-09-21 Mimicking pancreatic malignancy: a systemic sarcoidosis Zhang, Li-Na Xue, Qing-Liang Wang, Jian-Xin Ann Saudi Med Case Report Systemic sarcoidosis that initially presents as a pancreatic mass has rarely been reported. A 47-year-old man presented with idiopathic epigastric abdominal pain. Abdominal CT showed multiple enlarged lymph nodes in the retroperitoneal area and a suspected tumor mass in the pancreatic head region. The preliminary diagnosis was celiac metastasis of a pancreatic malignancy. The definitive diagnosis was systemic sarcoidosis, which was supported by granulomas on histology, clinical radiographic findings, and clinical response to steroids. A review of published reports on sarcoidosis presenting initially as a pancreatic or celiac mass from the Chinese biomedical database (1978–2010) is included. King Faisal Specialist Hospital and Research Centre 2014 /pmc/articles/PMC6074940/ /pubmed/24658558 http://dx.doi.org/10.5144/0256-4947.2014.70 Text en Copyright © 2014, Annals of Saudi Medicine This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Zhang, Li-Na
Xue, Qing-Liang
Wang, Jian-Xin
Mimicking pancreatic malignancy: a systemic sarcoidosis
title Mimicking pancreatic malignancy: a systemic sarcoidosis
title_full Mimicking pancreatic malignancy: a systemic sarcoidosis
title_fullStr Mimicking pancreatic malignancy: a systemic sarcoidosis
title_full_unstemmed Mimicking pancreatic malignancy: a systemic sarcoidosis
title_short Mimicking pancreatic malignancy: a systemic sarcoidosis
title_sort mimicking pancreatic malignancy: a systemic sarcoidosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074940/
https://www.ncbi.nlm.nih.gov/pubmed/24658558
http://dx.doi.org/10.5144/0256-4947.2014.70
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